Sensing Chromosome Bi-Orientation by Spatial Separation of Aurora B Kinase from Kinetochore Substrates

被引:439
作者
Liu, Dan [1 ]
Vader, Gerben [2 ]
Vromans, Martijn J. M. [2 ]
Lampson, Michael A. [1 ]
Lens, Susanne M. A. [2 ]
机构
[1] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
[2] Univ Med Ctr, Dept Med Oncol, NL-3584 CG Utrecht, Netherlands
基金
美国国家卫生研究院;
关键词
MICROTUBULE ATTACHMENT; CLEAVAGE FURROW; CELL-DIVISION; SPINDLE; ANAPHASE; COMPLEX; LOCALIZATION; CYTOKINESIS; MECHANISMS; CHECKPOINT;
D O I
10.1126/science.1167000
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Successful cell division requires that chromosomes attach to opposite poles of the mitotic spindle (bi-orientation). Aurora B kinase regulates chromosome-spindle attachments by phosphorylating kinetochore substrates that bind microtubules. Centromere tension stabilizes bi-oriented attachments, but how physical forces are translated into signaling at individual centromeres is unknown. Using fluorescence resonance energy transfer-based biosensors to measure localized phosphorylation dynamics in living cells, we found that phosphorylation of an Aurora B substrate at the kinetochore depended on its distance from the kinase at the inner centromere. Furthermore, repositioning Aurora B closer to the kinetochore prevented stabilization of bi-oriented attachments and activated the spindle checkpoint. Thus, centromere tension can be sensed by increased spatial separation of Aurora B from kinetochore substrates, which reduces phosphorylation and stabilizes kinetochore microtubules.
引用
收藏
页码:1350 / 1353
页数:4
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